(Q45300857)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16641246%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

CA150 expression delays striatal cell death in overexpression and knock-in conditions for mutant huntingtin neurotoxicity (English)

1 reference

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20 January 2020

1 reference

1 reference

1 reference

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4

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20 January 2020

Diana Zala

3

1 reference

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20 January 2020

Nicole Déglon

10

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20 January 2020

Christian Neri

11

1 reference

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20 January 2020

6

Etienne Régulier

1 reference

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20 January 2020

author name string

Margarita Arango

1

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20 January 2020

Sébastien Holbert

2

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20 January 2020

James Pearson

5

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20 January 2020

Ashwani Kumar Thakur

7

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20 January 2020

Patrick Aebischer

8

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20 January 2020

Ronald Wetzel

9

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20 January 2020

language of work or name

English

0 references

publication date

1 April 2006

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20 January 2020

published in

Journal of Neuroscience

1 reference

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20 January 2020

volume

26

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20 January 2020

issue

17

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20 January 2020

page(s)

4649-4659

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Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology

20 January 2020

cites work

1 reference

12 December 2020

Transcriptional cofactor CA150 regulates RNA polymerase II elongation in a TATA-box-dependent manner

1 reference

12 December 2020

Self-inactivating lentiviral vectors with enhanced transgene expression as potential gene transfer system in Parkinson's disease

1 reference

12 December 2020

The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription

1 reference

12 December 2020

Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells

1 reference

12 December 2020

Neurological abnormalities in a knock-in mouse model of Huntington's disease

1 reference

12 December 2020

The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis

1 reference

12 December 2020

Loss of normal huntingtin function: new developments in Huntington's disease research

1 reference

12 December 2020

Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity

1 reference

12 December 2020

Solubilization and disaggregation of polyglutamine peptides

1 reference

12 December 2020

Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease.

1 reference

12 December 2020

Polyglutamine aggregation behavior in vitro supports a recruitment mechanism of cytotoxicity

1 reference

12 December 2020

The transcription elongation factor CA150 interacts with RNA polymerase II and the pre-mRNA splicing factor SF1

1 reference

12 December 2020

Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila

1 reference

12 December 2020

Trinucleotide repeats: mechanisms and pathophysiology

1 reference

12 December 2020

PIASy, a nuclear matrix-associated SUMO E3 ligase, represses LEF1 activity by sequestration into nuclear bodies

1 reference

12 December 2020

Huntingtin is present in the nucleus, interacts with the transcriptional corepressor C-terminal binding protein, and represses transcription

1 reference

12 December 2020

Interaction of Huntington disease protein with transcriptional activator Sp1

1 reference

12 December 2020

HIP1 and HIP12 display differential binding to F-actin, AP2, and clathrin. Identification of a novel interaction with clathrin light chain

1 reference

12 December 2020

Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice

1 reference

12 December 2020

Huntingtin inclusions do not deplete polyglutamine-containing transcription factors in HD mice

1 reference

12 December 2020

Lentiviral-mediated delivery of mutant huntingtin in the striatum of rats induces a selective neuropathology modulated by polyglutamine repeat size, huntingtin expression levels, and protein length.

1 reference

12 December 2020

Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease

1 reference

12 December 2020

Amyloid-like features of polyglutamine aggregates and their assembly kinetics

1 reference

12 December 2020

Early transcriptional profiles in huntingtin-inducible striatal cells by microarray analyses

1 reference

12 December 2020

Hyperphosphorylated C-terminal repeat domain-associating proteins in the nuclear proteome link transcription to DNA/chromatin modification and RNA processing

1 reference

12 December 2020

Mutational analysis of the structural organization of polyglutamine aggregates

1 reference

12 December 2020

Cell death triggered by polyglutamine-expanded huntingtin in a neuronal cell line is associated with degradation of CREB-binding protein

1 reference

12 December 2020

Multiply attenuated, self-inactivating lentiviral vectors efficiently deliver and express genes for extended periods of time in adult rat cardiomyocytes in vivo.

1 reference

12 December 2020

Transcriptional abnormalities in Huntington disease

1 reference

12 December 2020

Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India

1 reference

12 December 2020

Stimulation of NeuroD activity by huntingtin and huntingtin-associated proteins HAP1 and MLK2

1 reference

12 December 2020

Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes

1 reference

12 December 2020

Disruption of Axonal Transport by Loss of Huntingtin or Expression of Pathogenic PolyQ Proteins in Drosophila

1 reference

12 December 2020

Neuropathogenic forms of huntingtin and androgen receptor inhibit fast axonal transport

1 reference

12 December 2020

Huntingtin bodies sequester vesicle-associated proteins by a polyproline-dependent interaction.

1 reference

12 December 2020

Neuroprotection by transforming growth factor-beta1 involves activation of nuclear factor-kappaB through phosphatidylinositol-3-OH kinase/Akt and mitogen-activated protein kinase-extracellular-signal regulated kinase1,2 signaling pathways.

1 reference

12 December 2020

Seeding specificity in amyloid growth induced by heterologous fibrils

1 reference

12 December 2020

Nuclear-targeting of mutant huntingtin fragments produces Huntington's disease-like phenotypes in transgenic mice

1 reference

12 December 2020

Cellular toxicity of polyglutamine expansion proteins: mechanism of transcription factor deactivation

1 reference

12 December 2020

Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules

1 reference

12 December 2020

PIASy represses TRIF-induced ISRE and NF-kappaB activation but not apoptosis.

1 reference

12 December 2020

Huntingtin and its role in neuronal degeneration

1 reference

12 December 2020

A protein interaction network links GIT1, an enhancer of huntingtin aggregation, to Huntington's disease

1 reference

12 December 2020

The WW domain-containing proteins interact with the early spliceosome and participate in pre-mRNA splicing in vivo

1 reference

12 December 2020

Huntingtin and the molecular pathogenesis of Huntington's disease. Fourth in molecular medicine review series

1 reference

12 December 2020

Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death

1 reference

12 December 2020

FF domains of CA150 bind transcription and splicing factors through multiple weak interactions

1 reference

12 December 2020

Polyglutamine expansion of huntingtin impairs its nuclear export

1 reference

12 December 2020

Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation

1 reference

12 December 2020

Pathological cell-cell interactions elicited by a neuropathogenic form of mutant Huntingtin contribute to cortical pathogenesis in HD mice.

1 reference

12 December 2020

Compounds blocking mutant huntingtin toxicity identified using a Huntington's disease neuronal cell model

1 reference

12 December 2020

Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment

1 reference

12 December 2020

Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease

1 reference

12 December 2020

Neuropeptide Y, somatostatin, and reduced nicotinamide adenine dinucleotide phosphate diaphorase in the human striatum: a combined immunocytochemical and enzyme histochemical study.

1 reference

12 December 2020

Bregma, lambda and the interaural midpoint in stereotaxic surgery with rats of different sex, strain and weight

1 reference

12 December 2020

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

12 December 2020

Recombination-mediated PCR-directed plasmid construction in vivo in yeast

1 reference

12 December 2020

CA150, a nuclear protein associated with the RNA polymerase II holoenzyme, is involved in Tat-activated human immunodeficiency virus type 1 transcription

1 reference

12 December 2020

Nuclear inclusions in glutamine repeat disorders: are they pernicious, coincidental, or beneficial?

1 reference

12 December 2020

Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

1 reference

12 December 2020

Transgenic mice in the study of polyglutamine repeat expansion diseases.

1 reference

12 December 2020

10.1523/JNEUROSCI.5409-05.2006

Identifiers

DOI

1 reference

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20 January 2020

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20 January 2020

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